GapMind for catabolism of small carbon sources

 

Alignments for a candidate for araZsh in Acidovorax sp. GW101-3H11

Align Inner-membrane translocator (characterized, see rationale)
to candidate Ac3H11_608 L-arabinose transport system permease protein (TC 3.A.1.2.2)

Query= uniprot:A0KWY7
         (320 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_608
          Length = 409

 Score =  110 bits (275), Expect = 6e-29
 Identities = 104/366 (28%), Positives = 171/366 (46%), Gaps = 77/366 (21%)

Query: 15  LLLTMFLVGTFQFDGFASGRVV-----TNLLRDNAFLLITALGMTLVIISGGIDLSVGAV 69
           L+  + ++G FQ+     G ++     TNL+  N++++I ALGM LVI++G IDLSVG+V
Sbjct: 41  LITLVAIMGFFQY--MTEGTLMQPLNLTNLVLQNSYIVIMALGMLLVIVAGHIDLSVGSV 98

Query: 70  IALSGVVTSLLITEYQWHPLLAFVVILPLGTLFGALMGTIIHVYKLQPFIVTLAGMFLAR 129
               G + ++L+ EY WH + A +V L  G L GA+ G+ +   ++  FIVTLAGM + +
Sbjct: 99  CGFIGALAAVLMVEYNWHFVPATLVCLLCGGLIGAIQGSFVAFSRIPSFIVTLAGMLVFK 158

Query: 130 GLATTL-------------------------SEESIAIDHPFYDAVAEMSIALPG----- 159
           GLA  L                         S E + +      A    ++A+ G     
Sbjct: 159 GLALALLAGQSVGPFPSAFQMLSSGFIPDLFSVEGLRMTSLLLGAAVAAALAVGGLRQRA 218

Query: 160 ----NGALDLSSLIFILFFVIIAVVMHYTRFGTNVYAIGGNQHSAELMGISI-------A 208
               +G     + +FI   V+   ++ Y  F   + +  G  +   +M + I       +
Sbjct: 219 NRLRHGVQTEPAGLFIARTVVFGGLLVY--FSYLLASYKGLPNVLIVMALLIVLFDFVTS 276

Query: 209 KTTIS--IYAI--SSFLATLAGIV---FTFYTF---------SGYALGA----------I 242
           +TTI   IYA+  +   A L+GI     T Y F         +G    A          +
Sbjct: 277 RTTIGRRIYAMGGNEKAAKLSGIKTERLTLYAFINMGVLAALAGLVFAARLNTATPKAGL 336

Query: 243 GVELDAIAAVVIGGTLLTGGSGFVLGTVLGVILMGVIQTYITFDGSLSSWWTKIVIGLLL 302
           G ELD IAA  IGG   +GG G V+G V+G  +MGV+   ++  G +   + +++ G++L
Sbjct: 337 GFELDVIAACFIGGASASGGVGKVMGAVIGAFVMGVMNNGMSILG-IGIDYQQVIKGVVL 395

Query: 303 FFFILL 308
              +L+
Sbjct: 396 LAAVLV 401


Lambda     K      H
   0.330    0.145    0.424 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 395
Number of extensions: 24
Number of successful extensions: 2
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 320
Length of database: 409
Length adjustment: 29
Effective length of query: 291
Effective length of database: 380
Effective search space:   110580
Effective search space used:   110580
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.8 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory